Device recall
Z-2866-2011: MEDRAD Avanta Fluid Management Injection System, Catalog numbers: AVA 500 TABL…
FDA device recall · Class II · Medrad Inc
Key facts
| Recall number (Z-number) | Z-2866-2011 |
|---|---|
| Recall event | 59167 |
| Product | MEDRAD Avanta Fluid Management Injection System, Catalog numbers: AVA 500 TABL, AVA 500 PEDL Product Usage: Administration of intravascular radio-opaque contrast media and common flushing solutions during angiographic procedures. |
| Product code | DXT |
| Recalling firm | Medrad Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 5, 2012 |
| 510(k) numbers | K050456 |
| FEI number | 2520313 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database